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The Top 5 Biosimilars Articles for the Week of March 4
The Center for Biosimilars® recaps the top news for the week of March 4, 2019.
Transcript:
Hi, I’m Samantha DiGrande for The Center for Biosimilars®, your resource for clinical, regulatory, business, and policy news in the rapidly changing world of biosimilars.
Here are the top 5 biosimilars articles for the week of March 4.
Number 5: The FDA has approved a subcutaneously administered version of the brand-name trastuzumab, Herceptin.
Number 4: Mylan revealed in its recent earnings call that it had an initial advisory meeting with the FDA regarding a proposed biosimilar referencing the brand-name Botox.
Number 3: During the European Crohn’s and Colitis Organisation’s14th Congress, held in Copenhagen, Denmark, researchers presented on real-world switches from reference infliximab to biosimilar CT-P13.
Number 2: Eli Lilly and Company is introducing a lower-priced authorized generic of its insulin lispro injection in the United States.
Number 1: FDA Commissioner Scott Gottlieb, MD, will be stepping down from his post in 1 month.
Finally, last week, our e-newsletter asked how important you think employers are to the US biosimilars market.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
President Trump Signs Executive Order to Bring Down Drug Prices
April 16th 2025To help bring down sky-high drug prices, President Donald Trump signed an executive order pushing for faster biosimilar development, more transparency, and tougher rules on pharmacy benefit managers—aiming to save billions and make meds more affordable for everyone.
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
Latest Biosimilar Deals Signal Growth Across Immunology, Oncology Markets
April 14th 2025During Q1 2025, pharmaceutical companies accelerated biosimilar expansion through strategic acquisitions and partnerships in hopes of boosting patient access to lower-cost treatments in immunology and oncology.
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
